A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519248



Internal ID15446541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94631195..94634130hg38UCSC Ensembl
Innerchr11:94364361..94367296hg19UCSC Ensembl
Innerchr11:94004009..94006944hg18UCSC Ensembl
Innerchr11:94004009..94006944hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382936
hg192936
hg182936
hg172936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696740
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519248
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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